CLASS II ONGOING Drug recall · Reported 4 Mar 2026 · FDA Enforcement Report

Vista Gel Hypromellose USP 0.3% w/v recalled by Wizcure Pharmaa Private

Wizcure Pharmaa Private is recalling Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, Wizcure, distributed nationwide in the US. The recall was initiated on 31 Dec 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots

NDC77790-002

Quantity recalled17,280 cartons

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number: D-0347-2026
FDA event ID: 98253
Recalling firm: Wizcure Pharmaa Private, Bhiwadi, N/A
Brand: Vista Hypromellose Dry Eye Relief
Manufacturer: Red Wedding LLC
Classification: Class II
Status: Ongoing
Recall initiated: 31 Dec 2025
FDA classified: 25 Feb 2026
Reported: 4 Mar 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Sterility
Drug class: Eye Drops

Timeline

31 Dec 2025	Recall initiated by company
25 Feb 2026	Classified by FDA	+56 days
4 Mar 2026	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 10 ml. (1/3 fl. oz), Wizcure Pharmaa PVT. LTD, H-881, Phase-3, RIICO Industrial Area, Bhiwadi-301019, India, Manufactured for and distributed by: hi-health, 15207 N. 75th Street, Suite #104, Scottsdale, AZ, 85260, NDC 77790-002-10.

Where it was distributed

Distributed Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.

Which lots are affected?

All lots

Where was it sold?

Distributed Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 98253

This product is part of a recall event; the main page for the event is BioGlo Fluorescein Sodium Ophthalmic Strips recalled.

Reported	Class	Recall	Company	Reason	Where
4 Mar 2026	CLASS II	BioGlo Fluorescein Sodium Ophthalmic Strips recalled	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026	CLASS II	Bio Glo Fluorescein Sodium Ophthalmic Strips recalled	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026	CLASS II	Vista Tears Polyethylene Glycol 400 0.4% w/v recalled	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026	CLASS II	Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution recalledVista Gonio Eye Lubricant	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026	CLASS II	Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops recalledVista Meibo Tears Propylene Glycol 0.6% W/v Advanced Dry Eye Relief Lubricating Drops 10 Ml	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026	CLASS II	CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) recalledC20h10na2o5 Fluorescein Sodium Ophthalmic Strips	Wizcure Pharmaa Private	Sterility	Nationwide

More recalls from Wizcure Pharmaa Private

All 7

Reported	Class	Recall	Company	Reason	Where
4 Mar 2026Drug	CLASS II	CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) recalledC20h10na2o5 Fluorescein Sodium Ophthalmic Strips	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026Drug	CLASS II	Vista Meibo Tears Propylene Glycol 0.6% w/v Eye Drops recalledVista Meibo Tears Propylene Glycol 0.6% W/v Advanced Dry Eye Relief Lubricating Drops 10 Ml	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026Drug	CLASS II	Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution recalledVista Gonio Eye Lubricant	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026Drug	CLASS II	Vista Tears Polyethylene Glycol 400 0.4% w/v recalled	Wizcure Pharmaa Private	Sterility	Nationwide
4 Mar 2026Drug	CLASS II	Bio Glo Fluorescein Sodium Ophthalmic Strips recalled	Wizcure Pharmaa Private	Sterility	Nationwide

Other Hypromellose recalls

All 6

Reported	Class	Recall	Company	Reason	Where
29 Jul 2026Drug	CLASS II	Rohto Cooling Eye Drops All-in-one (hypromellose recalledRohto	Rohto-Mentholatum (Vietnam)	Sterility	Nationwide
29 Jul 2026Drug	CLASS II	Rohto Cooling Eye Drops Digi Eye (hypromellose recalledRohto Digi-eye	Rohto-Mentholatum (Vietnam)	Sterility	Nationwide
6 May 2026Drug	CLASS II	Systane, Lubricant Eye Gel, Night Gel, Sterile, Processed recalledSystane	Alcon Research	Sterility	Nationwide
6 May 2026Drug	CLASS II	GenTeal Tears, Lubricant Eye Gel, Sterile recalled by Alcon ResearchGenteal Tears	Alcon Research	Sterility	Nationwide
4 Mar 2026Drug	CLASS II	Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution recalledVista Gonio Eye Lubricant	Wizcure Pharmaa Private	Sterility	Nationwide